rs1057518201

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1057518201(-;-)

Make rs1057518201(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

2081637

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs1057518201
dbSNP (classic)	rs1057518201
ClinGen	rs1057518201
ebi	rs1057518201
HLI	rs1057518201
Exac	rs1057518201
Gnomad	rs1057518201
Varsome	rs1057518201
LitVar	rs1057518201
Map	rs1057518201
PheGenI	rs1057518201
Biobank	rs1057518201
1000 genomes	rs1057518201
hgdp	rs1057518201
ensembl	rs1057518201
geneview	rs1057518201
scholar	rs1057518201
google	rs1057518201
pharmgkb	rs1057518201
gwascentral	rs1057518201
openSNP	rs1057518201
23andMe	rs1057518201
SNPshot	rs1057518201
SNPdbe	rs1057518201
MSV3d	rs1057518201
GWAS Ctlg	rs1057518201

Max Magnitude

0

ClinVar
Risk	rs1057518201(-;-)
Alt	rs1057518201(-;-)
Reference	Rs1057518201(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TSC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.2131638delC
CLNSRC
CLNACC	RCV000414407.1,